scholarly journals Regulation of Ammonia Homeostasis by the Ammonium Transporter AmtA in Dictyostelium discoideum

2007 ◽  
Vol 6 (12) ◽  
pp. 2419-2428 ◽  
Author(s):  
Ryuji Yoshino ◽  
Takahiro Morio ◽  
Yoko Yamada ◽  
Hidekazu Kuwayama ◽  
Masazumi Sameshima ◽  
...  

ABSTRACT Ammonia has been shown to function as a morphogen at multiple steps during the development of the cellular slime mold Dictyostelium discoideum; however, it is largely unknown how intracellular ammonia levels are controlled. In the Dictyostelium genome, there are five genes that encode putative ammonium transporters: amtA, amtB, amtC, rhgA, and rhgB. Here, we show that AmtA regulates ammonia homeostasis during growth and development. We found that cells lacking amtA had increased levels of ammonia/ammonium, whereas their extracellular ammonia/ammonium levels were highly decreased. These results suggest that AmtA mediates the excretion of ammonium. In support of a role for AmtA in ammonia homeostasis, AmtA mRNA is expressed throughout the life cycle, and its expression level increases during development. Importantly, AmtA-mediated ammonia homeostasis is critical for many developmental processes. amtA − cells are more sensitive to NH4Cl than wild-type cells in inhibition of chemotaxis toward cyclic AMP and of formation of multicellular aggregates. Furthermore, even in the absence of exogenously added ammonia, we found that amtA − cells produced many small fruiting bodies and that the viability and germination of amtA − spores were dramatically compromised. Taken together, our data clearly demonstrate that AmtA regulates ammonia homeostasis and plays important roles in multiple developmental processes in Dictyostelium.

CYTOLOGIA ◽  
1988 ◽  
Vol 53 (2) ◽  
pp. 337-340 ◽  
Author(s):  
Yohichi Hashimoto ◽  
Reiko Nakamura ◽  
Takeo Muroyama ◽  
Takuzo Yamada

1971 ◽  
Vol 49 (8) ◽  
pp. 1163-1177 ◽  
Author(s):  
Donald J. McQueen

The mechanics of a short-term interspecific competitive situation for two species of cellular slime mold, Dictyostelium discoideum and Polysphondylium pallidum, were assessed experimentally, modelled mathematically, and linked together to form a computer model, the predictions of which were tested. Five major components in the model were exploitation, toxic interference, effect of physical factors or external forces, availability of resources, and number of potential competitors engaged in exploitation and interference. The exploitation component depended upon time required for spore germination, rate and form of amoeba colony expansion, time required for fruiting body production, and rate and form of fruiting body colony expansion.Both species interfered with the other's ability to form fruiting bodies. In mixed cultures, D. discoideum amoebae divided and consumed food between 9° and 27 °C but did not produce fruiting bodies above 24 °C. In mixed cultures, P. pallidum amoebae divided and consumed food between 18° and 37 °C but did not produce fruiting bodies below 24 °C. Temperature altered the parameter values of all subcomponents contributing to exploitation and interference. Numbers altered interference ability. A computer model for predicting area occupied by fruiting bodies of both species was used to run 324 simulations and was accurate in 90.1% of the cases.


2006 ◽  
Vol 5 (10) ◽  
pp. 1820-1825 ◽  
Author(s):  
Nathaniel Whitney ◽  
Lacey J. Pearson ◽  
Ryan Lunsford ◽  
Lisa McGill ◽  
Richard H. Gomer ◽  
...  

ABSTRACT The Dictyostelium rbrA gene encodes a putative Ariadne ubiquitin ligase. rbrA − cells form defective slugs that cannot phototax. Prestalk cell numbers are reduced in rbrA − slugs, and these prestalk cells do not localize to the tip of slugs. Chimeric slugs containing wild-type cells could phototax and form fruiting bodies.


1989 ◽  
Vol 67 (10) ◽  
pp. 712-718 ◽  
Author(s):  
S. Ramagopal

This study documents the presence of three acidic proteins, A1 (pI 4.95), A2 (pI 4.85), and A3 (pI 4.70), in Dictyostelium discoideum ribosomes. All three proteins showed an apparent molecular mass of 13 000 by two-dimensional, sodium dodecyl sulfate gel electrophoresis. They were selectively released by treatment of ribosomes with 50% ethanol – 1 M NH4Cl. The amino acid compositions of A1, A2, and A3 were identical and indicated a predominant amount of alanine. All the above properties are shared by Escherichia coli proteins L7 and L12 and acidic ribosomal proteins in many eukaryotes. Unlike other eukaryotic systems, the acidic proteins of D. discoideum were found associated with the 40S rather than the 60S ribosomal subunit. Acidic proteins analogous in size and electrophoretic mobility to those of D. discoideum were also detected in several other cellular slime mold strains. Not one of the cellular slime mold acidic proteins reacted with antibodies to E. coli proteins L7 and L12 in immunodiffusion tests. In D. discoideum, the distribution of acidic proteins was altered during development. Amoebae contained all three proteins. In spores, A, was absent and the relative amounts of A2 and A3 were lower than in amoebae. In addition, nine other acidic ribosomal proteins exhibited differences between vegetative amoebae and spores.Key words: acidic ribosomal proteins, development, cellular slime mold, L7 and L12 proteins, two-dimensional gel electrophoresis.


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